A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p
- 1 October 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (4) , 924-927
- https://doi.org/10.1086/514892
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Identification of a hot spot for microdeletions in patients with X- linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Human Molecular Genetics, 1996
- HLA Class II-Associated Genetic Susceptibility in Idiopathic Progressive Sensorineural Hearing LossAnnals of Otology, Rhinology & Laryngology, 1996
- Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4Science, 1995
- A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalHuman Molecular Genetics, 1994
- Quantitative Trait Locus for Reading Disability on Chromosome 6Science, 1994
- In situ hybridization localizes the human OTF3 to chromosome 6p21.3→p22 and OTF3L to 12p13Cytogenetic and Genome Research, 1993
- Genetic Epidemiology of Hearing ImpairmentAnnals of the New York Academy of Sciences, 1991
- The human α2(XI) collagen gene (COL11A2) maps to the centromeric border of the major histocompatibility complex on chromosome 6Genomics, 1989
- A simple and efficient non-organic procedure for the isolation of genomic DNA from bloodNucleic Acids Research, 1989
- Cerebral LateralizationArchives of Neurology, 1985